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Search results for: filamentous bacteria
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1555</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: filamentous bacteria</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1555</span> Epiphytic Growth on Filamentous Bacteria Found in Activated Sludge: A Morphological Approach</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Thobela%20Conco">Thobela Conco</a>, <a href="https://publications.waset.org/abstracts/search?q=Sheena%20Kumari"> Sheena Kumari</a>, <a href="https://publications.waset.org/abstracts/search?q=Thor%20Stenstrom"> Thor Stenstrom</a>, <a href="https://publications.waset.org/abstracts/search?q=Simona%20Rosetti"> Simona Rosetti</a>, <a href="https://publications.waset.org/abstracts/search?q=Valter%20Tandoi"> Valter Tandoi</a>, <a href="https://publications.waset.org/abstracts/search?q=Faizal%20Bux"> Faizal Bux</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Filamentous bacteria are well documented as causative agents of bulking and foaming in the biological wastewater treatment process. These filamentous bacteria are however closely associated with other non-filamentous organism forming a micro-niche. Among these specific epiphytic bacteria attach to filaments in the consortium of organisms that make up the floc. Neither the eco-physiological role of the epiphytes nor the nature of the interaction between the epiphytic bacteria and the filament hosts they colonize is well understood and in need of in-depth investigations. The focus of this presentation is on the interaction between the epiphytic bacteria and the filament host. Samples from the activated sludge treatment have been repeatedly collected from several wastewater treatment plants in KwaZulu Natal. Extensive investigations have been performed with SEM and TEM electron microscopy, Polarized Light Microscopy with Congo red staining, and Thioflavin T staining to document the interaction. SEM was used to document the morphology of both the filament host and their epiphytes counterparts with the focus on the interface/point of contact between the two, while the main focus of the TEM investigations with the higher magnification aimed to document the ultra-structure features of two organisms relating to the interaction. The interaction of the perpendicular attachment partly seems to be governed by the physiological status of the filaments. The attachment further seems to trigger a response in the filaments with distinct internal visible structures at the attachment sites. It is postulated that these structures most likely are amyloid fibrils. Amyloid fibrils may play an overarching role in different types of attachments and has earlier been noted to play a significant role in biofilm formation in activated sludge. They also play a medical role in degenerative diseases such as Alzheimer’s and Diabetes. Further studies aims to define the eco-physiological role of amyloid fibrils in filamentous bacteria, based on their observed presence at interaction sites in this study. This will also relate to additional findings where selectivity within the species of epiphytes attaching to the selected filaments has been noted. The practical implications of the research findings is still to be determined, but the ecophysiological interaction between two closely associated species or groups may have significant impact in the future understanding of wastewater treatment processes and broaden existing knowledge on population dynamics. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=activated%20sludge" title="activated sludge">activated sludge</a>, <a href="https://publications.waset.org/abstracts/search?q=amyloid%20proteins" title=" amyloid proteins"> amyloid proteins</a>, <a href="https://publications.waset.org/abstracts/search?q=epiphytic%20bacteria" title=" epiphytic bacteria"> epiphytic bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=filamentous%20bacteria" title=" filamentous bacteria"> filamentous bacteria</a> </p> <a href="https://publications.waset.org/abstracts/35469/epiphytic-growth-on-filamentous-bacteria-found-in-activated-sludge-a-morphological-approach" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/35469.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">427</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1554</span> Impact of Activated Sludge Bulking and Foaming on the Quality of Kuwait's Irrigation Water</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abdallah%20Abusam">Abdallah Abusam</a>, <a href="https://publications.waset.org/abstracts/search?q=Andrzej%20Mydlarczyk"> Andrzej Mydlarczyk</a>, <a href="https://publications.waset.org/abstracts/search?q=Fadila%20Al-Salameen"> Fadila Al-Salameen</a>, <a href="https://publications.waset.org/abstracts/search?q=Moh%20Elmuntasir%20Ahmed"> Moh Elmuntasir Ahmed</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Treated municipal wastewater produced in Kuwait is used mainly in agricultural and greenery landscape irrigations. However, there are strong doubts that severe sludge bulking and foaming problems, particularly during winter seasons, may render the treated wastewater to be unsuitable for irrigation purposes. To assess the impact of sludge bulking and foaming problems on the quality of treated effluents, samples were collected weekly for nine months (January to September 2014) from the secondary effluents, tertiary effluents and sludge-mixed liquor streams of the two plants that severely suffer from sludge bulking and foaming problems. Dominant filamentous bacteria were identified and quantified using a molecular method called VIT (Vermicon Identification Technology). Quality of the treated effluents was determined according to water and wastewater standard methods. Obtained results were then statistically analyzed and compared to irrigation water standards. Statistical results indicated that secondary effluents were greatly impacted by sludge bulking and foaming problems, while tertiary effluents were slightly affected. This finding highlights the importance of having tertiary treatment units in plants that encountering sludge bulking and foaming problems. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=agriculture" title="agriculture">agriculture</a>, <a href="https://publications.waset.org/abstracts/search?q=filamentous%20bacteria" title=" filamentous bacteria"> filamentous bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=reclamation" title=" reclamation"> reclamation</a>, <a href="https://publications.waset.org/abstracts/search?q=reuse" title=" reuse"> reuse</a>, <a href="https://publications.waset.org/abstracts/search?q=wastewater" title=" wastewater"> wastewater</a> </p> <a href="https://publications.waset.org/abstracts/60154/impact-of-activated-sludge-bulking-and-foaming-on-the-quality-of-kuwaits-irrigation-water" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/60154.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">269</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1553</span> Enhanced Enzymes Production through Immobilization of Filamentous Fungi</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zhanara%20B.%20Suleimenova">Zhanara B. Suleimenova</a>, <a href="https://publications.waset.org/abstracts/search?q=Zhazira%20K.%20Saduyeva"> Zhazira K. Saduyeva</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Filamentous fungi are major producers of enzymes that have important applications in the food and beverage industries. The overall objective of this research is a strain improvement technology for efficient industrial enzymes production. The new way of filamentous fungi cultivation method has been developed. Such technology prolong producers’ cultivation period up to 60 days and create the opportunity to obtain enzymes repeatedly in every 2-3 days of fungal cultivation. This method is based on immobilizing enzymes producers with solid support in submerged conditions of growth. Immobilizing has a range of advantages: Decreasing the price of the final product, absence of foreign substances, controlled process of enzyme-genesis, ability of various enzymes simultaneous production, etc. Design of proposed technology gives the opportunity to increase the activity of immobilized cells culture filtrate comparing to free cells, growing in periodic culture conditions. Thus, proposed research focuses on new, more versatile, microorganisms capable of squeezing more end-products as well as proposed cultivation technology led to increased enzymatic productivity by several times. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=filamentous%20fungi" title="filamentous fungi">filamentous fungi</a>, <a href="https://publications.waset.org/abstracts/search?q=immobilization" title=" immobilization"> immobilization</a>, <a href="https://publications.waset.org/abstracts/search?q=industrial%20enzymes%20production" title=" industrial enzymes production"> industrial enzymes production</a>, <a href="https://publications.waset.org/abstracts/search?q=strain%20improvement" title=" strain improvement "> strain improvement </a> </p> <a href="https://publications.waset.org/abstracts/27195/enhanced-enzymes-production-through-immobilization-of-filamentous-fungi" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/27195.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">359</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1552</span> Selection Effects on the Molecular and Abiotic Evolution of Antibiotic Resistance</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abishek%20Rajkumar">Abishek Rajkumar</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Antibiotic resistance can occur naturally given the selective pressure placed on antibiotics. Within a large population of bacteria, there is a significant chance that some of those bacteria can develop resistance via mutations or genetic recombination. However, a growing public health concern has arisen over the fact that antibiotic resistance has increased significantly over the past few decades. This is because humans have been over-consuming and producing antibiotics, which has ultimately accelerated the antibiotic resistance seen in these bacteria. The product of all of this is an ongoing race between scientists and the bacteria as bacteria continue to develop resistance, which creates even more demand for an antibiotic that can still terminate the newly resistant strain of bacteria. This paper will focus on a myriad of aspects of antibiotic resistance in bacteria starting with how it occurs on a molecular level and then focusing on the antibiotic concentrations and how they affect the resistance and fitness seen in bacteria. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=antibiotic" title="antibiotic">antibiotic</a>, <a href="https://publications.waset.org/abstracts/search?q=molecular" title=" molecular"> molecular</a>, <a href="https://publications.waset.org/abstracts/search?q=mutation" title=" mutation"> mutation</a>, <a href="https://publications.waset.org/abstracts/search?q=resistance" title=" resistance"> resistance</a> </p> <a href="https://publications.waset.org/abstracts/66066/selection-effects-on-the-molecular-and-abiotic-evolution-of-antibiotic-resistance" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/66066.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">323</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1551</span> Evaluation of Antimicrobial Activity of Different Dithiolethiones</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zehour%20Rahmani">Zehour Rahmani</a>, <a href="https://publications.waset.org/abstracts/search?q=Messouda%20Dekmouche"> Messouda Dekmouche</a>, <a href="https://publications.waset.org/abstracts/search?q=Mohamed%20Hadjadj"> Mohamed Hadjadj</a>, <a href="https://publications.waset.org/abstracts/search?q=Mokhtar%20Saidi"> Mokhtar Saidi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In the last decades of the nineteenth century, the study of disease – causing microorganisms became concentrated on bacteria and largely institutionalized. In earlier years, the scientists interested in bacteria had originally been chemists like Pasteur, physicists like Tyndall, or botanists like Cohn and ward. For this reason, the objective of this research was to evaluate the potential of some dithiolethiones on standard microorganism strains as well as multi-drug resistant bacteria, which were isolated from hospitals. Recent studies have demonstrated, that several dithiolethione compounds, particularly (3H-1,2-dithiole-3-thione), exhibit the biological activities against several bacteria. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bacteria" title="bacteria">bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=dithiolethiones" title=" dithiolethiones"> dithiolethiones</a>, <a href="https://publications.waset.org/abstracts/search?q=microorganism" title=" microorganism"> microorganism</a>, <a href="https://publications.waset.org/abstracts/search?q=potential" title=" potential "> potential </a> </p> <a href="https://publications.waset.org/abstracts/39624/evaluation-of-antimicrobial-activity-of-different-dithiolethiones" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/39624.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">318</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1550</span> Ethanol and Biomass Production from Spent Sulfite Liquor by Filamentous Fungi</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20T.%20Asadollahzadeh">M. T. Asadollahzadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Ghasemian"> A. Ghasemian</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20R.%20Saraeian"> A. R. Saraeian</a>, <a href="https://publications.waset.org/abstracts/search?q=H.%20Resalati"> H. Resalati</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20R.%20Lennartsson"> P. R. Lennartsson</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20J.%20Taherzadeh"> M. J. Taherzadeh</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Since filamentous fungi are capable of assimilating several types of sugars (hexoses and pentoses), they are potential candidates for bioconversion of spent sulfite liquor (SSL). Three filamentous fungi such as <em>Aspergillus oryzae</em>, <em>Mucor indicus</em>, and <em>Rhizopus oryzae</em> were investigated in this work. The SSL was diluted in order to obtain concentrations of 50, 60, 70, 80, and 90% and supplemented with two types of nutrients. The results from cultivations in shake flask showed that <em>A. oryzae</em> and <em>M. indicus</em> were not able to grow in pure SSL and SSL90% while <em>R. oryzae</em> could grow only in SSL50% and SSL60%. Cultivation with <em>A. oryzae</em> resulted in the highest yield of produced fungal biomass, while <em>R. oryzae</em> cultivation resulted in the lowest fungal biomass yield. Although, the mediums containing yeast extract, (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub>, KH<sub>2</sub>PO<sub>4</sub>, CaCl<sub>2</sub>∙2H<sub>2</sub>O, and MgSO<sub>4</sub>∙7H<sub>2</sub>O as nutrients supplementations produced higher fungal biomass compared to the mediums containing NH<sub>4</sub>H<sub>2</sub>PO<sub>4</sub> and ammonia, but there was no significant difference between two types of nutrients in terms of sugars and acetic acid consumption rate. The sugars consumption in <em>M. indicus</em> cultivation was faster than <em>A. oryzae</em> and <em>R. oryzae</em> cultivation. Acetic acid present in SSL was completely consumed during cultivation of all fungi. <em>M. indicus</em> was the best and fastest ethanol producer from SSL among the fungi examined, when yeast extract and salts were used as nutrients supplementations. Furthermore, no further improvement in ethanol concentration and rate of sugars consumption was obtained in medium supplemented with NH<sub>4</sub>H<sub>2</sub>PO<sub>4</sub> and ammonia compared to medium containing yeast extract, (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub>, KH<sub>2</sub>PO<sub>4</sub>, CaCl<sub>2</sub>∙2H<sub>2</sub>O, and MgSO<sub>4</sub>∙7H<sub>2</sub>O. On the other hand, the higher dilution of SSL resulted in a better fermentability, and better consumption of sugars and acetic acid. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ethanol" title="ethanol">ethanol</a>, <a href="https://publications.waset.org/abstracts/search?q=filamentous%20fungi" title=" filamentous fungi"> filamentous fungi</a>, <a href="https://publications.waset.org/abstracts/search?q=fungal%20biomass" title=" fungal biomass"> fungal biomass</a>, <a href="https://publications.waset.org/abstracts/search?q=spent%20sulfite%20liquor" title=" spent sulfite liquor"> spent sulfite liquor</a> </p> <a href="https://publications.waset.org/abstracts/53168/ethanol-and-biomass-production-from-spent-sulfite-liquor-by-filamentous-fungi" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/53168.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">254</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1549</span> Developing a Set of Primers Targeting Chondroitin Ac Lyase Gene for Specific and Sensitive Detection of Flavobacterium Columnare, a Causative Agent of Freshwater Columnaris</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mahmoud%20%20Mabrok">Mahmoud Mabrok</a>, <a href="https://publications.waset.org/abstracts/search?q=Channarong%20Rodkhum"> Channarong Rodkhum</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Flavobacterium columanre is one of the devastating pathogen that causes noticeable economic losses in freshwater cultured fish. Like other filamentous bacteria, F. columanre tends to aggregate and fluctuate to all kind of media, thus revealing obstacles in recognition of its colonies. Since the molecular typing is the only fundamental tool for rapid and precise detection of this pathgen. The present study developed a species-specific PCR assay based on cslA unique gene of F. columnare. The cslA gene sequences of 13 F. columnare, strains retrieved from gene bank database, were aligned to identify a conserved homologous segment prior to primers design. The new primers yielded amplicons of 287 bp from F. columnare strains but not from relevant or other pathogens, unlike to other published set that showed no specificity and cross-reactivity with F. indicum. The primers were sensitive and detected as few as 7 CFUs of bacteria and 3 pg of gDNA template. The sensitivity was reduced ten times when using tissue samples. These primers precisely defined all field isolates in a double-blind study, proposing their applicable use for field detection. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Columnaris%20infection" title="Columnaris infection">Columnaris infection</a>, <a href="https://publications.waset.org/abstracts/search?q=cslA%20gene" title=" cslA gene"> cslA gene</a>, <a href="https://publications.waset.org/abstracts/search?q=Flavobacterium%20columnare" title=" Flavobacterium columnare"> Flavobacterium columnare</a>, <a href="https://publications.waset.org/abstracts/search?q=PCR" title=" PCR"> PCR</a> </p> <a href="https://publications.waset.org/abstracts/123300/developing-a-set-of-primers-targeting-chondroitin-ac-lyase-gene-for-specific-and-sensitive-detection-of-flavobacterium-columnare-a-causative-agent-of-freshwater-columnaris" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/123300.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">127</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1548</span> Extracellular Laccase Production by Co-culture between Galactomyces reesii IFO 10823 and Filamentous Fungal Strains Isolated from Fungus Comb Using Natural Inducer</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=P.%20Chaijak">P. Chaijak</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Lertworapreecha"> M. Lertworapreecha</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Sukkasem"> C. Sukkasem</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Extracellular laccases are copper-containing microbial enzymes with many industrial biotechnological applications. This study evaluated the ability of nutrients in coconut coir to enhance the yield of extracellular laccase of <em>Galactomyces reesii</em> IFO 10823 and develop a co-culture between this yeast and other filamentous fungi isolated from the fungus comb of <em>Macrotermes</em> sp. The co-culture between <em>G. reesii</em> IFO 10823 and <em>M. indicus</em> FJ-M-5 (G3) gave the highest activity at 580.20 U/mL. When grown in fermentation media prepared from coconut coir and distilled water at 70% of initial moisture without supplement addition, G3 produced extracellular laccase of 113.99 U/mL. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=extracellular%20laccase" title="extracellular laccase">extracellular laccase</a>, <a href="https://publications.waset.org/abstracts/search?q=production" title=" production"> production</a>, <a href="https://publications.waset.org/abstracts/search?q=yeast" title=" yeast"> yeast</a>, <a href="https://publications.waset.org/abstracts/search?q=natural%20inducer" title=" natural inducer"> natural inducer</a> </p> <a href="https://publications.waset.org/abstracts/65364/extracellular-laccase-production-by-co-culture-between-galactomyces-reesii-ifo-10823-and-filamentous-fungal-strains-isolated-from-fungus-comb-using-natural-inducer" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/65364.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">266</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1547</span> Investigating the Biosorption Potential of Indigenous Filamentous Fungi from Copperbelt Tailing Dams in Zambia with Copper and Cobalt Tolerance</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Leonce%20Dusengemungu">Leonce Dusengemungu</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Filamentous fungi indigenous to heavy metals (HMs) contaminated environments have a considerable biosorption potential yet are currently under-investigated in developing countries. In the work presented herein, the biosorption potential of three indigenous filamentous fungi (Aspergillus transmontanensis, Cladosporium cladosporioides, and Geotrichum candidum) isolated from copper and cobalt mining wasteland sites in Zambia's Copperbelt province was investigated. In Cu and Co tolerance tests, all the fungal isolates were shown to be tolerant, with mycelial growth at HMs concentrations of up to 7000 ppm. However, exposure to high Cu and Co concentrations hindered the growth of the three strains to varying degrees, resulting in reduced mycelial biomass (evidenced by loss of the infrared bands at 887 and 930 cm-1 of the 1,3-glucans backbone) as well as morphological alterations, sporulation, and pigment synthesis. In addition, gas chromatography-mass spectrometry characterization of the fungal biomass extracts allowed to detect changes in the chemical constituents upon exposure to HMs, with profiles poorer in maltol, 1,2-cyclopentadione, and n-hexadecanoic acid, and richer in furaldehydes. Biosorption tests showed that A. transmontanensis and G. candidum showed better performance as bioremediators than C. cladosporioides, with biosorption efficiencies of 1645, 1853 and 1253 ppm at pH 3, respectively, and may deserve further research in field conditions. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bioremediation" title="bioremediation">bioremediation</a>, <a href="https://publications.waset.org/abstracts/search?q=fungi" title=" fungi"> fungi</a>, <a href="https://publications.waset.org/abstracts/search?q=biosorption" title=" biosorption"> biosorption</a>, <a href="https://publications.waset.org/abstracts/search?q=heavy%20metal" title=" heavy metal"> heavy metal</a> </p> <a href="https://publications.waset.org/abstracts/175638/investigating-the-biosorption-potential-of-indigenous-filamentous-fungi-from-copperbelt-tailing-dams-in-zambia-with-copper-and-cobalt-tolerance" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/175638.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">64</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1546</span> Setting the Acceleration Test Conditions for Establishing the Expiration Date of Probiotics</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Myoyeon%20Kim">Myoyeon Kim</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The number of probiotics is various from product to product. The product must contain as many bacteria as the number of bacteria that claim because it greatly affects consumers' choices. It is very difficult to determine the number of viable bacteria with tests that proceed during the product development stage because the shelf life of lactic acid bacteria is mostly 18 to 24 months, and product development proceeds much faster than this. To predict the shelf life, a method of checking the number of viable bacteria was studied by shortening the time. The experiment was conducted with a total of 7 products including our products. The ongoing test stored at room temperature, the acceleration test stored at 30°C and 40°C were performed, and the number of bacteria was measured every two weeks. The number of viable bacteria stored at 30°C for 12 weeks was similar to the ongoing test when the shelf life was imminent. If it took more than 12 weeks, the product development schedule was postponed, so acceleration had no meaning. It was found that products stored at 40°C were unsuitable as acceleration test temperatures because the bacteria were almost killed within 4 to 8 weeks. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=probiotics" title="probiotics">probiotics</a>, <a href="https://publications.waset.org/abstracts/search?q=shelf-life" title=" shelf-life"> shelf-life</a>, <a href="https://publications.waset.org/abstracts/search?q=acceleration%20test" title=" acceleration test"> acceleration test</a>, <a href="https://publications.waset.org/abstracts/search?q=lactobacillus" title=" lactobacillus"> lactobacillus</a> </p> <a href="https://publications.waset.org/abstracts/188379/setting-the-acceleration-test-conditions-for-establishing-the-expiration-date-of-probiotics" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/188379.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">36</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1545</span> Effects of Bacteria on Levels of AFM1 in Phosphate Buffer at Different Level of Energy Source</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ali%20M.%20Elgerbi">Ali M. Elgerbi</a>, <a href="https://publications.waset.org/abstracts/search?q=Obied%20A.%20Alwan"> Obied A. Alwan</a>, <a href="https://publications.waset.org/abstracts/search?q=Al-Taher%20O.%20Alzwei"> Al-Taher O. Alzwei</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdurrahim%20A.%20Elouzi"> Abdurrahim A. Elouzi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The binding of AFM1 to bacteria in phosphate buffer solution depended on many factors such as: availability of energy, incubation period, species and strain of bacteria. Increase in concentration of sugar showed higher removal of AFM1 and faster than in phosphate buffer alone. With 1.0% glucose lactic acid bacteria and bifidobacteria showed toxin removal ranging from 7.7 to 39.7% whereas with 10.0% glucose the percentage removal was 21.8 to 45.4% at 96 hours of incubation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=aflatoxin%20M1" title="aflatoxin M1">aflatoxin M1</a>, <a href="https://publications.waset.org/abstracts/search?q=lactic%20acid%20bacteria" title=" lactic acid bacteria"> lactic acid bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=bifidobacteria" title=" bifidobacteria "> bifidobacteria </a>, <a href="https://publications.waset.org/abstracts/search?q=binding" title=" binding"> binding</a>, <a href="https://publications.waset.org/abstracts/search?q=phosphate%20buffer" title=" phosphate buffer "> phosphate buffer </a> </p> <a href="https://publications.waset.org/abstracts/19875/effects-of-bacteria-on-levels-of-afm1-in-phosphate-buffer-at-different-level-of-energy-source" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/19875.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">506</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1544</span> An Antifungal Peptide from Actinobacteria (Streptomyces Sp. TKJ2): Isolation and Partial Characterization</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abdelaziz%20Messis">Abdelaziz Messis</a>, <a href="https://publications.waset.org/abstracts/search?q=Azzeddine%20Bettache"> Azzeddine Bettache</a>, <a href="https://publications.waset.org/abstracts/search?q=Nawel%20Boucherba"> Nawel Boucherba</a>, <a href="https://publications.waset.org/abstracts/search?q=Said%20Benallaoua"> Said Benallaoua</a>, <a href="https://publications.waset.org/abstracts/search?q=Mouloud%20Kecha"> Mouloud Kecha</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Actinobacteria are of special biotechnological interest since they are known to produce chemically diverse compounds with a wide range of biological activity. This distinct clade of Gram-positve bacteria include some of the key antibiotic producers and are also sources of several bioactive compounds, established commercially a newly filamentous bacteria was recovered from Tikjda forest soil (Algeria) for its high antifungal activity against various pathogenic and phytopathogenic fungi. The nucleotide sequence of the 16S rRNA gene (1454 pb) of Streptomyces sp. TKJ2 exhibited close similarity (99 %) with other Streptomyces16S rRNA genes. Antifungal metabolite production of Streptomyces sp TKJ2 was evaluated using six different fermentation media. The extracellular products contained potent antifungal agents. Antifungal protein produced by Streptomyces sp. TKJ2 on PCA medium has been purified by ammonium sulfate precipitation, SPE column chromatography and high-performance liquid chromatography in a reverse-phase column. The UV chromatograms of the active fractions obtained at 214 nm by NanoLC-ESI-MS/MS have different molecular weights. The F20 Peptidic fraction obtained from culture filtrat of Streptomyces sp. TKJ2 precipitated at 30% of ammonium sulfate was selected for analysis by infusion ESI-MS which yielded a singly charged ion mass of 437.17 Da. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=actinobacteria" title="actinobacteria">actinobacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=antifungal%20protein" title=" antifungal protein"> antifungal protein</a>, <a href="https://publications.waset.org/abstracts/search?q=chromatography" title=" chromatography"> chromatography</a>, <a href="https://publications.waset.org/abstracts/search?q=Streptomyces" title=" Streptomyces "> Streptomyces </a> </p> <a href="https://publications.waset.org/abstracts/26624/an-antifungal-peptide-from-actinobacteria-streptomyces-sp-tkj2-isolation-and-partial-characterization" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/26624.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">383</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1543</span> Bacteria Removal from Wastewater by Electrocoagulation Process</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Boudjema%20Nouara">Boudjema Nouara</a>, <a href="https://publications.waset.org/abstracts/search?q=Mameri%20%20Nabil"> Mameri Nabil</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Bacteria have played an important role in water contamination as a consequence of organic pollution. In this study, an electrocoagulation process was adopted to remove fecal contamination and pathogenic bacteria from waste water. The effect of anode/cathodes materials as well as operating conditions for bacteria removal from water, such as current intensity and initial pH and temperature. The results indicated that the complete removal was achevied when using aluminium anode as anode at current intensity of 3A, initial pH of 7-8 and electrolysis time of 30 minutes. This process showed a bactericidal effect of 95 to 99% for the total and fecal coliforms and 99% to 100% for Eschercichia coli and fecal Streptococci. A decrease of 72% was recorded for sulphite-reducing Clostridia. Thus, this process has the potential to be one the options for treatment where high amount of bacteria in wastewater river. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bacteria" title="bacteria">bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=el%20Harrach%20river" title=" el Harrach river"> el Harrach river</a>, <a href="https://publications.waset.org/abstracts/search?q=electrocoagulation" title=" electrocoagulation"> electrocoagulation</a>, <a href="https://publications.waset.org/abstracts/search?q=wastewater" title=" wastewater"> wastewater</a>, <a href="https://publications.waset.org/abstracts/search?q=treatment" title=" treatment"> treatment</a> </p> <a href="https://publications.waset.org/abstracts/28065/bacteria-removal-from-wastewater-by-electrocoagulation-process" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/28065.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">496</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1542</span> Characterization of Biosurfactants Produced by Bacteria Degrading Gasoline</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ikram%20Kamal">Ikram Kamal</a>, <a href="https://publications.waset.org/abstracts/search?q=Mohamed%20Blaghen"> Mohamed Blaghen</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Biosurfactants are amphiphilic biological compounds consisting of hydrophobic and hydrophilic domains produced extracellularly or as part of the cell membrane by a variety of yeast, bacteria and filamentous fungi. Biosurfactant applications in the environmental industries are promising due to their biodegradability, low toxicity, and effectiveness in enhancing biodegradation and solubilization of low solubility compounds. Currently, the main application is for enhancement of oil recovery and hydrocarbon bioremediation due to their biodegradability and low critical micelle concentration (CMC). The use of biosurfactants has also been proposed for various industrial applications, such as in food additives, cosmetics, detergent formulations and in combinations with enzymes for wastewater treatment. In this study, we have investigated the potential of bacterial strains: Mannheimia haemolytica, Burkholderia cepacia and Serratia ficaria were collected aseptically from the lagoon Marchika (water and soil) in Nador, Morocco; for the production of biosurfactants. This study also aimed to optimize the biosurfactant production process by changing the variables that influence the type and amount of biosurfactant produced by these microorganisms such as: carbon sources and also other physical and chemical parameters such as temperature and pH. Emulsification index, methylene blue test, and thin layer chromatography (TLC) revealed the ability of strains used in this study to produce compounds that could emulsify gasoline. In addition, a GC/MS was used to separate and identify different biosurfactants purified. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biosurfactants" title="biosurfactants">biosurfactants</a>, <a href="https://publications.waset.org/abstracts/search?q=Mannheimia%20haemolytica" title=" Mannheimia haemolytica"> Mannheimia haemolytica</a>, <a href="https://publications.waset.org/abstracts/search?q=biodegradability" title=" biodegradability"> biodegradability</a>, <a href="https://publications.waset.org/abstracts/search?q=Burkholderia%20cepacia" title=" Burkholderia cepacia"> Burkholderia cepacia</a>, <a href="https://publications.waset.org/abstracts/search?q=Serratia%20ficaria" title=" Serratia ficaria"> Serratia ficaria</a> </p> <a href="https://publications.waset.org/abstracts/42419/characterization-of-biosurfactants-produced-by-bacteria-degrading-gasoline" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/42419.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">257</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1541</span> Isolation and Characterization of Indigenous Rhizosphere Bacteria Producing Gibberellin Acid from Local Soybeans in Three Different Areas of South Sulawesi</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Asmiaty%20Sahur">Asmiaty Sahur</a>, <a href="https://publications.waset.org/abstracts/search?q=Ambo%20Ala"> Ambo Ala</a>, <a href="https://publications.waset.org/abstracts/search?q=Baharuddin%20Patanjengi"> Baharuddin Patanjengi</a>, <a href="https://publications.waset.org/abstracts/search?q=Elkawakib%20Syam%27un"> Elkawakib Syam'un</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study aimed to isolate and characterize the indigenous Rhizosphere bacteria producing Gibberellin Acid as plant growth isolated from local soybean of three different areas in South Sulawesi, Indonesia. Several soil samples of soybean plants were collected from the Rhizosphere of local soybeans in three different areas of South Sulawesi such as Soppeng, Bone and Takalar. There were 56 isolates of bacteria were isolated and grouped into gram-positive bacteria and gram negative bacteria .There are 35 isolates produce a thick slime or slimy when cultured on media Natrium Broth and the remaining of those produced spores. The results showed that of potential bacterial isolated produced Gibberellin Acid in high concentration. The best isolate of Rhizosphere bacteria for the production of Gibberellin Acid is with concentration 2%. There are 4 isolates that had higher concentration are AKB 19 (4.67 mg/ml) followed by RKS 17 (3.80 mg/ml), RKS 25 (3.70 mg / ml) and RKS 24 (3.29 mg/ml) respectively. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=rhizosphere" title="rhizosphere">rhizosphere</a>, <a href="https://publications.waset.org/abstracts/search?q=bacteria" title=" bacteria"> bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=gibberellin%20acid" title=" gibberellin acid"> gibberellin acid</a>, <a href="https://publications.waset.org/abstracts/search?q=soybeans" title=" soybeans"> soybeans</a> </p> <a href="https://publications.waset.org/abstracts/35624/isolation-and-characterization-of-indigenous-rhizosphere-bacteria-producing-gibberellin-acid-from-local-soybeans-in-three-different-areas-of-south-sulawesi" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/35624.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">236</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1540</span> Influence of Culturing Conditions on Biomass Yield, Total Lipid and Fatty Acid Composition of Some Filamentous Fungi</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Alla%20V.%20Goncharova">Alla V. Goncharova</a>, <a href="https://publications.waset.org/abstracts/search?q=Tatyana%20A.%20Karpenyuk"> Tatyana A. Karpenyuk</a>, <a href="https://publications.waset.org/abstracts/search?q=Yana%20S.%20Tsurkan"> Yana S. Tsurkan</a>, <a href="https://publications.waset.org/abstracts/search?q=Rosa%20U.%20Beisembaeva"> Rosa U. Beisembaeva</a>, <a href="https://publications.waset.org/abstracts/search?q=Togzhan%20D.%20Mukasheva"> Togzhan D. Mukasheva</a>, <a href="https://publications.waset.org/abstracts/search?q=Ludmila%20V.%20Ignatova"> Ludmila V. Ignatova</a>, <a href="https://publications.waset.org/abstracts/search?q=Ramza%20Z.%20Berzhanova"> Ramza Z. Berzhanova </a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this work the effect of culturing conditions of filamentous fungi Penicillium raistrickii, Penicillium anatolicum, Fusarium sp. on biomass yield, the content of total lipids and fatty acids was studied. It has been established that in time the process of lipids accumulation correlated with biomass growth of cultures, reaching maximum values in stationary growth phase. Biomass yield and accumulation of general lipids was increased by adding zinc to the culture medium. The more intensive accumulation of biomass and general lipids was observed at temperature 18°C. Lowering the temperature of culturing has changed the ratio of saturated: Unsaturated fatty acids in the direction of increasing the latter. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biomass" title="biomass">biomass</a>, <a href="https://publications.waset.org/abstracts/search?q=culturing%20conditions" title=" culturing conditions"> culturing conditions</a>, <a href="https://publications.waset.org/abstracts/search?q=fungi" title=" fungi"> fungi</a>, <a href="https://publications.waset.org/abstracts/search?q=fatty%20acids%20%28FA%29" title=" fatty acids (FA)"> fatty acids (FA)</a>, <a href="https://publications.waset.org/abstracts/search?q=growth%20dynamics" title=" growth dynamics"> growth dynamics</a>, <a href="https://publications.waset.org/abstracts/search?q=lipids" title=" lipids"> lipids</a> </p> <a href="https://publications.waset.org/abstracts/10193/influence-of-culturing-conditions-on-biomass-yield-total-lipid-and-fatty-acid-composition-of-some-filamentous-fungi" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/10193.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">451</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1539</span> The Effect of Bacteria on Mercury's Biological Removal</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nastaran%20Soltani">Nastaran Soltani</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Heavy metals such as Mercury are toxic elements that enter the environment through different ways and endanger the environment, plants, animals, and humans’ health. Microbial activities reduce the amount of heavy metals. Therefore, an effective mechanism to eliminate heavy metals in the nature and factory slops, is using bacteria living in polluted areas. Karun River in Khuzestan Province in Iran has been always polluted by heavy metals as it is located among different industries in the region. This study was performed based on the data from sampling water and sediments of four stations across the river during the four seasons of a year. The isolation of resistant bacteria was performed through enrichment and direct cultivation in a solid medium containing mercury. Various bacteria such as Pseudomonas sp., Serratia Marcescens, and E.coli were identified as mercury-resistant bacteria. The power of these bacteria to remove mercury varied from 28% to 86%, with strongest power belonging to Pseudomonas sp. isolated in spring making a good candidate to be used for mercury biological removal from factory slops. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bacteria" title="bacteria">bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=Karun%20River" title=" Karun River"> Karun River</a>, <a href="https://publications.waset.org/abstracts/search?q=mercury" title=" mercury"> mercury</a>, <a href="https://publications.waset.org/abstracts/search?q=biological%20removal" title=" biological removal"> biological removal</a>, <a href="https://publications.waset.org/abstracts/search?q=mercury-resistant" title=" mercury-resistant"> mercury-resistant</a> </p> <a href="https://publications.waset.org/abstracts/46736/the-effect-of-bacteria-on-mercurys-biological-removal" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/46736.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">286</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1538</span> Examining the Presence of Heterotrophic Aerobic Bacteria (HAB), and Sulphate Reducing Bacteria (SRB) in Some Types of Water from the City of Tripoli, Libya</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abdulsalam.%20I.%20Rafida">Abdulsalam. I. Rafida</a>, <a href="https://publications.waset.org/abstracts/search?q=Marwa.%20F.%20Elalem"> Marwa. F. Elalem</a>, <a href="https://publications.waset.org/abstracts/search?q=Hasna.%20E.%20Alemam"> Hasna. E. Alemam</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study aimed at testing the various types of water in some areas of the city of Tripoli, Libya for the presence of Heterotrophic Aerobic Bacteria (HAB), and anaerobic Sulphate Reducing Bacteria (SRB). The water samples under investigation included rainwater accumulating on the ground, sewage water (from the city sewage treatment station, sulphate water from natural therapy swimming sites), and sea water (i.e. sea water exposed to pollution by untreated sewage water, and unpolluted sea water from specific locations). A total of 20 samples have been collected distributed as follows: rain water (8 samples), sewage water (6 samples), and sea water (6 samples). An up-to-date method for estimation has been used featuring readymade solutions i.e. (BARTTM test for HAB and BARTTM test for SRB). However, with the exception of one rain water sample, the results have indicated that the target bacteria have been present in all samples. Regarding HAB bacteria the samples have shown a maximum average of 7.0 x 106 cfu/ml featuring sewage and rain water and a minimum average of 1.8 x 104 cuf/ml featuring unpolluted sea water collected from a specific location. As for SRB bacteria; a maximum average of 7.0 x 105 cfu/ml has been shown by sewage and rain water and a minimum average of 1.8 x 104 cfu/ml by sewage and sea water. The above results highlight the relationship between pollution and the presence of bacteria in water particularly water collected from specific locations, and also the presence of bacteria as the result of the use of water provided that a suitable environment exists for its growth. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=heterotrophic%20aerobic%20bacteria%20%28HAB%29" title="heterotrophic aerobic bacteria (HAB)">heterotrophic aerobic bacteria (HAB)</a>, <a href="https://publications.waset.org/abstracts/search?q=sulphate%20reducing%20bacteria%20%28SRB%29" title=" sulphate reducing bacteria (SRB)"> sulphate reducing bacteria (SRB)</a>, <a href="https://publications.waset.org/abstracts/search?q=water" title=" water"> water</a>, <a href="https://publications.waset.org/abstracts/search?q=environmental%20sciences" title=" environmental sciences"> environmental sciences</a> </p> <a href="https://publications.waset.org/abstracts/19642/examining-the-presence-of-heterotrophic-aerobic-bacteria-hab-and-sulphate-reducing-bacteria-srb-in-some-types-of-water-from-the-city-of-tripoli-libya" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/19642.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">491</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1537</span> Isolation, Screening and Identification of Frog Cutaneous Bacteria for Anti-Batrachochytrium dendrobatidis Activity</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Adria%20Rae%20Abigail%20R.%20Eda">Adria Rae Abigail R. Eda</a>, <a href="https://publications.waset.org/abstracts/search?q=Arvin%20C.%20Diesmos"> Arvin C. Diesmos</a>, <a href="https://publications.waset.org/abstracts/search?q=Vance%20T.%20Vredenburg"> Vance T. Vredenburg</a>, <a href="https://publications.waset.org/abstracts/search?q=Merab%20A.%20Chan"> Merab A. Chan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Mitigating strategies using symbiotic cutaneous bacteria is one of the major concerns in the conservation of amphibian population. Batrachochytrium dendrobatidis is the causative agent of chytridiomycosis associated with mass mortality and amphibian extinctions worldwide. In the Philippines, there is a lack of study on the cutaneous bacteria of Philippine amphibians that may have beneficial effects to ward off the deadly fungal infection. In this study, cutaneous bacteria from frogs were isolated and examined for anti-B. dendrobatidis activity. Eight species of frogs were collected at Mt. Palay-palay Mataas na Gulod National Park in Cavite, a site positive for the presence of B. dendrobatidis. Bacteria were isolated from the skin of frogs by swabbing the surfaces of the body and inoculated in Reasoner´s 2A (R2A) agar. Isolated bacteria were tested for potential inhibitory properties against B. dendrobatidis through zoospore inhibition assay. Results showed that frog cutaneous bacteria significantly inhibited the growth of B. dendrobatidis in vitro. By means of 16S rRNA gene primers, the anti-B. dendrobatidis bacteria were identified to be Enterobacter sp., Alcaligenes faecalis and Pseudomonas sp. Cutaneous bacteria namely Enterobacter sp. (isolates PLd33 and PCv4) and Pseudomonas (isolate PLd31) remarkably cleared the growth of B. dendrobatidis zoospore in 1% tryptone agar. Therefore, frog cutaneous bacteria inhibited B. dendrobatidis in vitro and could possibly contribute to the immunity and defense of frogs against the lethal chytridiomycosis. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Batrachochytrium%20dendrobatidis" title="Batrachochytrium dendrobatidis">Batrachochytrium dendrobatidis</a>, <a href="https://publications.waset.org/abstracts/search?q=cutaneous%20bacteria" title=" cutaneous bacteria"> cutaneous bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=frogs" title=" frogs"> frogs</a>, <a href="https://publications.waset.org/abstracts/search?q=zoospore%20inhibition%20assay" title=" zoospore inhibition assay"> zoospore inhibition assay</a> </p> <a href="https://publications.waset.org/abstracts/21413/isolation-screening-and-identification-of-frog-cutaneous-bacteria-for-anti-batrachochytrium-dendrobatidis-activity" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/21413.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">454</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1536</span> Lactobacillus sp. Isolates Slaughterhouse Waste as Probiotics for Broilers</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nourmalita%20Safitri%20Ningsih">Nourmalita Safitri Ningsih</a>, <a href="https://publications.waset.org/abstracts/search?q=Ridwan"> Ridwan</a>, <a href="https://publications.waset.org/abstracts/search?q=Iqri%20Puspa%20Yunanda"> Iqri Puspa Yunanda</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The aim of this study was to utilize the waste from slaughterhouses for chicken feed ingredients is probiotic. Livestock waste produced by livestock activities such as feces, urine, food remains, as well as water from livestock and cage cleaning. The process starts with the isolation of bacteria. Rumen fluid is taken at Slaughterhouse Giwangan, Yogyakarta. Isolation of Lactobacillus ruminus is done by using de Mann Rogosa Sharpe (MRS) medium. In the sample showed a rod-shaped bacteria are streaked onto an agar plates. After it was incubated at 37ºC for 48 hours, after which it is observed. The observation of these lactic acid bacteria it will show a clear zone at about the colony. These bacterial colonies are white, round, small, shiny on the agar plate mikroenkapsul In the manufacturing process carried out by the method of freeze dried using skim milk in addition capsulated material. Then the results of these capsulated bacteria are mixed with feed for livestock. The results from the mixing of capsulated bacteria in feed are to increase the quality of animal feed so as to provide a good effect on livestock. Scanning electron microscope testing we have done show the results of bacteria have been shrouded in skim milk. It can protect the bacteria so it is more durable in use. The observation of the bacteria showed a sheath on Lactobacillus sp. Preservation of bacteria in this way makes the bacteria more durable for use. As well as skim milk can protect bacteria that are resistant to the outside environment. Results of probiotics in chicken feed showed significant weight gain in chickens. Calculation Anova (P <0.005) shows the average chicken given probiotics her weight increased. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chicken" title="chicken">chicken</a>, <a href="https://publications.waset.org/abstracts/search?q=probiotics" title=" probiotics"> probiotics</a>, <a href="https://publications.waset.org/abstracts/search?q=waste" title=" waste"> waste</a>, <a href="https://publications.waset.org/abstracts/search?q=Lactobacillus%20sp" title=" Lactobacillus sp"> Lactobacillus sp</a>, <a href="https://publications.waset.org/abstracts/search?q=bacteria" title=" bacteria"> bacteria</a> </p> <a href="https://publications.waset.org/abstracts/44218/lactobacillus-sp-isolates-slaughterhouse-waste-as-probiotics-for-broilers" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/44218.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">319</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1535</span> Study on the Heavy Oil Degradation Performance and Kinetics of Immobilized Bacteria on Modified Zeolite</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Xiao%20L%20Dai">Xiao L Dai</a>, <a href="https://publications.waset.org/abstracts/search?q=Wen%20X%20Wei"> Wen X Wei</a>, <a href="https://publications.waset.org/abstracts/search?q=Shuo%20Wang"> Shuo Wang</a>, <a href="https://publications.waset.org/abstracts/search?q=Jia%20B%20Li"> Jia B Li</a>, <a href="https://publications.waset.org/abstracts/search?q=Yan%20Wei"> Yan Wei</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Heavy oil pollution generated from both natural and anthropogenic sources could cause significant damages to the ecological environment, due to the toxicity of some of its constituents. Nowadays, microbial remediation is becoming a promising technology to treat oil pollution owing to its low cost and prevention of secondary pollution; microorganisms are key players in the process. Compared to the free microorganisms, immobilized microorganisms possess several advantages, including high metabolic activity rates, strong resistance to toxic chemicals and natural competition with the indigenous microorganisms, and effective resistance to washing away (in open water system). Many immobilized microorganisms have been successfully used for bioremediation of heavy oil pollution. Considering the broad choices, low cost, simple process, large specific surface area and less impact on microbial activity, modified zeolite were selected as a bio-carrier for bacteria immobilization. Three strains of heavy oil-degrading bacteria Bacillus sp. DL-13, Brevibacillus sp. DL-1 and Acinetobacter sp. DL-34 were immobilized on the modified zeolite under mild conditions, and the bacterial load (bacteria /modified zeolite) was 1.12 mg/g, 1.11 mg/g, and 1.13 mg/g, respectively. SEM results showed that the bacteria mainly adsorbed on the surface or punctured in the void of modified zeolite. The heavy oil degradation efficiency of immobilized bacteria was 62.96%, higher than that of the free bacteria (59.83%). The heavy oil degradation process of immobilized bacteria accords with the first-order reaction equation, and the reaction rate constant is 0.1483 d⁻¹, which was significantly higher than the free bacteria (0.1123 d⁻¹), suggesting that the immobilized bacteria can rapidly start up the heavy oil degradation and has a high activity of heavy oil degradation. The results suggested that immobilized bacteria are promising technology for bioremediation of oil pollution. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=heavy%20oil%20pollution" title="heavy oil pollution">heavy oil pollution</a>, <a href="https://publications.waset.org/abstracts/search?q=microbial%20remediation" title=" microbial remediation"> microbial remediation</a>, <a href="https://publications.waset.org/abstracts/search?q=modified%20zeolite" title=" modified zeolite"> modified zeolite</a>, <a href="https://publications.waset.org/abstracts/search?q=immobilized%20bacteria" title=" immobilized bacteria"> immobilized bacteria</a> </p> <a href="https://publications.waset.org/abstracts/110195/study-on-the-heavy-oil-degradation-performance-and-kinetics-of-immobilized-bacteria-on-modified-zeolite" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/110195.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">150</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1534</span> Biodiversity of Plants Rhizosphere and Rhizoplane Bacteria in the Presence of Petroleum Hydrocarbons</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Togzhan%20D.%20Mukasheva">Togzhan D. Mukasheva</a>, <a href="https://publications.waset.org/abstracts/search?q=Anel%20A.%20Omirbekova"> Anel A. Omirbekova</a>, <a href="https://publications.waset.org/abstracts/search?q=Raikhan%20S.%20Sydykbekova"> Raikhan S. Sydykbekova</a>, <a href="https://publications.waset.org/abstracts/search?q=Ramza%20Zh.%20Berzhanova"> Ramza Zh. Berzhanova</a>, <a href="https://publications.waset.org/abstracts/search?q=Lyudmila%20V.%20Ignatova"> Lyudmila V. Ignatova</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Following plants-barley (Hordeum sativum), alfalfa (Medicago sativa), grass mixture (red fescue-75%, long-term ryegrass - 20% Kentucky bluegrass - 10%), oilseed rape (Brassica napus biennis), resistant to growth in the contaminated soil with oil content of 15.8 g / kg 25.9 g / kg soil were used. Analysis of the population showed that the oil pollution reduces the number of bacteria in the rhizosphere and rhizoplane of plants and enhances the amount of spore-forming bacteria and saprotrophic micromycetes. It was shown that regardless of the plant, dominance of Pseudomonas and Bacillus genera bacteria was typical for the rhizosphere and rhizoplane of plants. The frequency of bacteria of these genera was more than 60%. Oil pollution changes the ratio of occurrence of various types of bacteria in the rhizosphere and rhizoplane of plants. Besides the Pseudomonas and Bacillus genera, in the presence of hydrocarbons in the root zone of plants dominant and most typical were the representatives of the Mycobacterium and Rhodococcus genera. Together the number was between 62% to 72%. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=pollution" title="pollution">pollution</a>, <a href="https://publications.waset.org/abstracts/search?q=root%20system" title=" root system"> root system</a>, <a href="https://publications.waset.org/abstracts/search?q=micromycetes" title=" micromycetes"> micromycetes</a>, <a href="https://publications.waset.org/abstracts/search?q=identification" title=" identification"> identification</a> </p> <a href="https://publications.waset.org/abstracts/10208/biodiversity-of-plants-rhizosphere-and-rhizoplane-bacteria-in-the-presence-of-petroleum-hydrocarbons" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/10208.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">499</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1533</span> Phylogenetic Characterization of Atrazine-Degrading Bacteria Isolated from Agricultural Soil in Eastern Thailand</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sawangjit%20Sopid">Sawangjit Sopid</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study sugarcane field soils with a long history of atrazine application in Chachoengsao and Chonburi provinces have been explored for their potential of atrazine biodegradation. For the atrazine degrading bacteria isolation, the soils used in this study named ACS and ACB were inoculated in MS-medium containing atrazine. Six short rod and gram-negative bacterial isolates, which were able to use this herbicide as a sole source of nitrogen, were isolated and named as ACS1, ACB1, ACB3, ACB4, ACB5 and ACB6. From the 16S rDNA nucleotide sequence analysis, the isolated bacteria ACS1 and ACB4 were identified as Rhizobium sp. with 89.1-98.7% nucleotide identity, ACB1 and ACB5 were identified as Stenotrophomonas sp. with 91.0-92.8% nucleotide identity, whereas ACB3 and ACB6 were Klebsiella sp. with 97.4-97.8% nucleotide identity. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=atrazine-degrading%20bacteria" title="atrazine-degrading bacteria">atrazine-degrading bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=bioremediation" title=" bioremediation"> bioremediation</a>, <a href="https://publications.waset.org/abstracts/search?q=Thai%20isolates" title=" Thai isolates"> Thai isolates</a>, <a href="https://publications.waset.org/abstracts/search?q=bacteria" title=" bacteria"> bacteria</a> </p> <a href="https://publications.waset.org/abstracts/12599/phylogenetic-characterization-of-atrazine-degrading-bacteria-isolated-from-agricultural-soil-in-eastern-thailand" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/12599.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">888</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1532</span> Characterization of Bacteria by a Nondestructive Sample Preparation Method in a TEM System</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=J.%20Shiue">J. Shiue</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20H.%20Chen"> I. H. Chen</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20W.%20Y.%20Chiu"> S. W. Y. Chiu</a>, <a href="https://publications.waset.org/abstracts/search?q=Y.%20L.%20Wang"> Y. L. Wang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this work, we present a nondestructive method to characterize bacteria in a TEM system. Unlike the conventional TEM specimen preparation method, which needs to thin the specimen in a destructive way, or spread the samples on a tiny millimeter sized carbon grid, our method is easy to operate without the need of sample pretreatment. With a specially designed transparent chip that allows the electron beam to pass through, and a custom made chip holder to fit into a standard TEM sample holder, the bacteria specimen can be easily prepared on the chip without any pretreatment, and then be observed under TEM. The centimeter-sized chip is covered with Au nanoparticles in the surface as the markers which allow the bacteria to be observed easily on the chip. We demonstrate the success of our method by using E. coli as an example, and show that high-resolution TEM images of E. coli can be obtained with the method presented. Some E. coli morphology characteristics imaged using this method are also presented. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bacteria" title="bacteria">bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=chip" title=" chip"> chip</a>, <a href="https://publications.waset.org/abstracts/search?q=nanoparticles" title=" nanoparticles"> nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=TEM" title=" TEM"> TEM</a> </p> <a href="https://publications.waset.org/abstracts/54896/characterization-of-bacteria-by-a-nondestructive-sample-preparation-method-in-a-tem-system" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/54896.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">314</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1531</span> On a Negative Relation between Bacterial Taxis and Turing Pattern Formation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Elragig">A. Elragig</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Townley"> S. Townley</a>, <a href="https://publications.waset.org/abstracts/search?q=H.%20Dreiwi"> H. Dreiwi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this paper we introduce a bacteria-leukocyte model with bacteria chemotaxsis. We assume that bacteria develop a tactic defense mechanism as a response to Leukocyte phagocytosis. We explore the effect of this tactic motion on Turing space in two parameter spaces. A fine tuning of bacterial chemotaxis shows a significant effect on developing a non-uniform steady state. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chemotaxis-diffusion%20driven%20instability" title="chemotaxis-diffusion driven instability">chemotaxis-diffusion driven instability</a>, <a href="https://publications.waset.org/abstracts/search?q=bacterial%20chemotaxis" title=" bacterial chemotaxis"> bacterial chemotaxis</a>, <a href="https://publications.waset.org/abstracts/search?q=mathematical%20biology" title=" mathematical biology"> mathematical biology</a>, <a href="https://publications.waset.org/abstracts/search?q=ecology" title=" ecology"> ecology</a> </p> <a href="https://publications.waset.org/abstracts/12873/on-a-negative-relation-between-bacterial-taxis-and-turing-pattern-formation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/12873.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">368</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1530</span> Encapsulated Bacteria In Polymer Composites For Bioremediation Applications </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mahsa%20Mafi">Mahsa Mafi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Encapsulation of Micrococcus Luteus (M. Luteus) in polymeric composites has been employed for the bioremediation, sequestration of metals and for the biodegradation of chemical pollutants and toxic components in waste water. Polymer composites in the form of nonwovens of nanofibers, or core/shell particles can provide a bacterial friendly environment for transfer of nutrients and metabolisms, with the least leakage of bacteria. M. Luteus is encapsulated in a hydrophilic core of poly (vinyl alcohol), following by synthesis or coating of a proper shell as a support to maintain the chemical and mechanical strength. The biological activity of bacteria is confirmed by Live/Dead analysis and agar plate tests. SEM and TEM analysis were utilized for morphological studies of polymer composites. As a result of the successful encapsulation of the alive bacteria in polymers, longer storage time in their functional state were achieved. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Polymer%20composites" title="Polymer composites">Polymer composites</a>, <a href="https://publications.waset.org/abstracts/search?q=Bacteria%20encapsulation" title=" Bacteria encapsulation"> Bacteria encapsulation</a>, <a href="https://publications.waset.org/abstracts/search?q=Bioremediation" title=" Bioremediation"> Bioremediation</a>, <a href="https://publications.waset.org/abstracts/search?q=Waste%20water%20treatment" title=" Waste water treatment"> Waste water treatment</a> </p> <a href="https://publications.waset.org/abstracts/120376/encapsulated-bacteria-in-polymer-composites-for-bioremediation-applications" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/120376.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">137</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1529</span> Different Formula of Mixed Bacteria as a Bio-Treatment for Sewage Wastewater</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=E.%20Marei">E. Marei</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Hammad"> A. Hammad</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Ismail"> S. Ismail</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20El-Gindy"> A. El-Gindy</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study aims to investigate the ability of different formula of mixed bacteria as a biological treatments of wastewater after primary treatment as a bio-treatment and bio-removal and bio-adsorbent of different heavy metals in natural circumstances. The wastewater was collected from Sarpium forest site-Ismailia Governorate, Egypt. These treatments were mixture of free cells and mixture of immobilized cells of different bacteria. These different formulas of mixed bacteria were prepared under Lab. condition. The obtained data indicated that, as a result of wastewater bio-treatment, the removal rate was found to be 76.92 and 76.70% for biological oxygen demand, 79.78 and 71.07% for chemical oxygen demand, 32.45 and 36.84 % for ammonia nitrogen as well as 91.67 and 50.0% for phosphate after 24 and 28 hrs with mixed free cells and mixed immobilized cells, respectively. Moreover, the bio-removals of different heavy metals were found to reach 90.0 and 50. 0% for Cu ion, 98.0 and 98.5% for Fe ion, 97.0 and 99.3% for Mn ion, 90.0 and 90.0% Pb, 80.0% and 75.0% for Zn ion after 24 and 28 hrs with mixed free cells and mixed immobilized cells, respectively. The results indicated that 13.86 and 17.43% of removal efficiency and reduction of total dissolved solids were achieved after 24 and 28 hrs with mixed free cells and mixed immobilized cells, respectively. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=wastewater%20%20bio-treatment" title="wastewater bio-treatment ">wastewater bio-treatment </a>, <a href="https://publications.waset.org/abstracts/search?q=bio-sorption%20heavy%20metals" title=" bio-sorption heavy metals"> bio-sorption heavy metals</a>, <a href="https://publications.waset.org/abstracts/search?q=biological%20desalination" title=" biological desalination"> biological desalination</a>, <a href="https://publications.waset.org/abstracts/search?q=immobilized%20bacteria" title=" immobilized bacteria"> immobilized bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=free%20cell%20bacteria" title=" free cell bacteria"> free cell bacteria</a> </p> <a href="https://publications.waset.org/abstracts/88568/different-formula-of-mixed-bacteria-as-a-bio-treatment-for-sewage-wastewater" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/88568.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">201</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1528</span> Bioremediation of Phenanthrene by Monocultures and Mixed Culture Bacteria Isolated from Contaminated Soil</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Fazilah">A. Fazilah</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Darah"> I. Darah</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Noraznawati"> I. Noraznawati</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Three different bacteria capable of degrading phenanthrene were isolated from hydrocarbon contaminated site. In this study, the phenanthrene-degrading activity by defined monoculture was determined and mixed culture was identified as <em>Acinetobacter</em> sp. P3d, <em>Bacillus </em>sp. P4a and <em>Pseudomonas</em> sp. P6. All bacteria were able to grow in a minimal salt medium saturated with phenanthrene as the sole source of carbon and energy. Phenanthrene degradation efficiencies by different combinations (consortia) of these bacteria were investigated and their phenanthrene degradation was evaluated by gas chromatography. Among the monocultures,<em> Pseudomonas</em> sp. P6 exhibited 58.71% activity compared to <em>Acinetobacter</em> sp. P3d and <em>Bacillus</em> sp. P4a which were 56.97% and 53.05%, respectively after 28 days of cultivation. All consortia showed high phenanthrene elimination which were 95.64, 79.37, 87.19, 79.21% for Consortia A, B, C and D, respectively. The results indicate that all of the bacteria isolated may effectively degrade target chemical and have a promising application in bioremediation of hydrocarbon contaminated soil purposes. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=phenanthrene" title="phenanthrene">phenanthrene</a>, <a href="https://publications.waset.org/abstracts/search?q=consortia" title=" consortia"> consortia</a>, <a href="https://publications.waset.org/abstracts/search?q=acinetobacter%20sp.%20P3d" title=" acinetobacter sp. P3d"> acinetobacter sp. P3d</a>, <a href="https://publications.waset.org/abstracts/search?q=bacillus%20sp.%20P4a" title=" bacillus sp. P4a"> bacillus sp. P4a</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas%20sp.%20P6" title=" pseudomonas sp. P6"> pseudomonas sp. P6</a> </p> <a href="https://publications.waset.org/abstracts/47580/bioremediation-of-phenanthrene-by-monocultures-and-mixed-culture-bacteria-isolated-from-contaminated-soil" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/47580.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">296</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1527</span> Using Electro-Biogrouting to Stabilize of Soft Soil</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hamed%20A.%20Keykha">Hamed A. Keykha</a>, <a href="https://publications.waset.org/abstracts/search?q=Hadi%20Miri"> Hadi Miri</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This paper describes a new method of soil stabilisation, electro-biogrouting (EBM), for improvement of soft soil with low hydraulic conductivity. This method uses an applied voltage gradient across the soil to induce the ions and bacteria cells through the soil matrix, resulting in CaCO3 precipitation and an increase of the soil shear strength in the process. The EBM were used effectively with two injection methods; bacteria injection and products of bacteria injection. The bacteria cells, calcium ions and urea were moved across the soil by electromigration and electro osmotic flow respectively. The products of bacteria (CO3-2) were moved by electromigration. The results showed that the undrained shear strength of the soil increased from 6 to 65 and 70 kPa for first and second injection method respectively. The injection of carbonate solution and calcium could be effectively flowed in the clay soil compare to injection of bacteria cells. The detection of CaCO3 percentage and its corresponding water content across the specimen showed that the increase of undrained shear strength relates to the deposit of calcite crystals between soil particles. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sporosarcina%20pasteurii" title="Sporosarcina pasteurii">Sporosarcina pasteurii</a>, <a href="https://publications.waset.org/abstracts/search?q=electrophoresis" title=" electrophoresis"> electrophoresis</a>, <a href="https://publications.waset.org/abstracts/search?q=electromigration" title=" electromigration"> electromigration</a>, <a href="https://publications.waset.org/abstracts/search?q=electroosmosis" title=" electroosmosis"> electroosmosis</a>, <a href="https://publications.waset.org/abstracts/search?q=biocement" title=" biocement"> biocement</a> </p> <a href="https://publications.waset.org/abstracts/23192/using-electro-biogrouting-to-stabilize-of-soft-soil" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/23192.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">528</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1526</span> Isolation of Biosurfactant Producing Spore-Forming Bacteria from Oman: Potential Applications in Bioremediation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Saif%20N.%20Al-Bahry">Saif N. Al-Bahry</a>, <a href="https://publications.waset.org/abstracts/search?q=Yahya%20M.%20Al-Wahaibi"> Yahya M. Al-Wahaibi</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdulkadir%20E.%20Elshafie"> Abdulkadir E. Elshafie</a>, <a href="https://publications.waset.org/abstracts/search?q=Ali%20S.%20Al-Bemani"> Ali S. Al-Bemani</a>, <a href="https://publications.waset.org/abstracts/search?q=Sanket%20J.%20Joshi"> Sanket J. Joshi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Environmental pollution is a global problem and best possible solution is identifying and utilizing native microorganisms. One possible application of microbial product -biosurfactant is in bioremediation of hydrocarbon contaminated sites. We have screened forty two different petroleum contaminated sites from Oman, for biosurfactant producing spore-forming bacterial isolates. Initial screening showed that out of 42 soil samples, three showed reduction in surface tension (ST) and interfacial tension (IFT) within 24h of incubation at 40°C. Out of those 3 soil samples, one was further selected for isolation of bacteria and 14 different bacteria were isolated in pure form. Of those 14 spore-forming, rod shaped bacteria, two showed highest reduction in ST and IFT in the range of 70mN/m to < 35mN/m and 26.69mN/m to < 9mN/m, respectively within 24h. These bacterial biosurfactants may be utilized for bioremediation of oil-spills. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bioremediation" title="bioremediation">bioremediation</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrocarbon%20pollution" title=" hydrocarbon pollution"> hydrocarbon pollution</a>, <a href="https://publications.waset.org/abstracts/search?q=spore-forming%20bacteria" title=" spore-forming bacteria"> spore-forming bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=bio-surfactant" title=" bio-surfactant"> bio-surfactant</a> </p> <a href="https://publications.waset.org/abstracts/3715/isolation-of-biosurfactant-producing-spore-forming-bacteria-from-oman-potential-applications-in-bioremediation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/3715.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">297</span> </span> </div> </div> <ul class="pagination"> <li class="page-item disabled"><span class="page-link">‹</span></li> <li class="page-item active"><span class="page-link">1</span></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=filamentous%20bacteria&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=filamentous%20bacteria&page=3">3</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=filamentous%20bacteria&page=4">4</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=filamentous%20bacteria&page=5">5</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=filamentous%20bacteria&page=6">6</a></li> 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